The biogenesis of β-lactamase enzymes

Author:

Kaderabkova Nikol1,Bharathwaj Manasa2,Furniss R. Christopher D.3,Gonzalez Diego4,Palmer Tracy5,Mavridou Despoina A.I.61ORCID

Affiliation:

1. Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas, USA

2. Centre to Impact AMR, Biomedicine Discovery Institute and Department of Microbiology, Monash University, Melbourne, Victoria, Australia

3. Science for Life Laboratory, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden

4. Laboratoire de Microbiologie, Institut de Biologie, Université de Neuchâtel, Neuchâtel, 2000, Switzerland

5. Microbes in Health and Disease, Newcastle University Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK

6. John Ring LaMontagne Center for Infectious Diseases, The University of Texas at Austin, Austin, Texas, USA

Abstract

The discovery of penicillin by Alexander Fleming marked a new era for modern medicine, allowing not only the treatment of infectious diseases, but also the safe performance of life-saving interventions, like surgery and chemotherapy. Unfortunately, resistance against penicillin, as well as more complex β-lactam antibiotics, has rapidly emerged since the introduction of these drugs in the clinic, and is largely driven by a single type of extra-cytoplasmic proteins, hydrolytic enzymes called β-lactamases. While the structures, biochemistry and epidemiology of these resistance determinants have been extensively characterized, their biogenesis, a complex process including multiple steps and involving several fundamental biochemical pathways, is rarely discussed. In this review, we provide a comprehensive overview of the journey of β-lactamases, from the moment they exit the ribosomal channel until they reach their final cellular destination as folded and active enzymes.

Publisher

Microbiology Society

Subject

Microbiology

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